Chemical structure
Cat.No.
Product Name
CAS no.
Target
Vinconate is an indolonaphthyridine derivative and can stimulate themuscariic acetylcholine receptor.
YN360456 5-Hydroxydecanoate sodium 71186-53-3
5-Hydroxydecanoate sodium is a selectiveATP-sensitive K+(KATP)channel blocker (IC50 of ~30μM). 5-Hydroxydecanoate sodium is a substrate for mitochondrial outer membrane acyl-CoA synthetase and has antioxidant activity.
YN380179 Moclobemide 71320-77-9
Moclobemide is a MAO-A (5-HT) inhibitor with IC50 of 6.1 μM.
YN1730072 Amisulpride 71675-85-9
Amisulpride is an atypical antipsychotic used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder.
Sp-cAMPS, a cAMP analog, is potent activator of cAMP-dependent PKA I and PKA II. Sp-cAMPS is also a potent, competitivephosphodiesterase (PDE3A) inhibitor with a Ki of 47.6 µM. Sp-cAMPS binds the PDE...
YN483897 Substance P, Free Acid 71977-09-8
Substance P, Free Acid is a native substance P analog, but shows no biological activity of substance P.
Spinosin ameliorated memory impairment induced through AβO, the serotonergic neurotransmitter system, and these effects were regulated, in part, through neuroprotective activity via the anti-inflammatory effects of Spinosin. Spinosin...
YN321795 β-Casomorphin, bovine 72122-62-4
β-Casomorphin, bovine (β-Casomorphin-7 (bovine) ) is aopioidpeptide with an IC50 of 14μM in an Opioid receptors binding assay.
YN371545 Apovincaminic acid hydrochlor... 72296-47-0
Apovincaminic acid hydrochloride salt is an orally active and brain-penetrant main active metabolite of Vinpocetine (VP). Apovincaminic acid hydrochloride salt exerts a neuroprotective type of action.
YN360234 Aniracetam 72432-10-1
Aniracetam is a nootropics and neuroprotective drug.
Miglustat (Zavesca, N‐butyldeoxynojirimycin, OGT 918) is an orally administered ceramide glucosyltransferase inhibitor which prevents the lysosomal accumulation of glucocerebroside.
YN320811 ICI 118,551 hydrochloride 72795-01-8
ICI 118,551 (hydrochloride) is a highly selectiveβ2 adrenergic receptorantagonist, with Kis of 0.7, 49.5 and 611nM for β2, β1 and β3 receptors, respectively.
YN321315 Tianeptine 72797-41-2
Tianeptine is an antidepressant agent that act as an atypical agonist of the μ-opioid receptor with clinically negligible effects on the δ- and κ-opioid receptors.
YN361060 Darodipine 72803-02-2
Darodipine (PY 108-068, PY-108068) is a potentcalcium channelantagonist.
CyPPA is a positive modulator ofhSK3 and hSK2, withEC50values of 14μM and 5.6μM, repectively. CyPPA is inactive on both hSK1 and hIK channels.
YN481181 1-(Anilinocarbonyl)proline 73096-22-7
1-(Anilinocarbonyl)proline can be used to identify dual action probes in a cell model of Huntington.
Effusol, a phenolic constituent fromJuncus effuses, exhibits potent scavenging activity for DPPH and ABTS radicals, with IC50 values of 79μM and 2.73μM, respectively. Effusol rescues CA1 LTP attenuated by corticost...
Rp-cAMPS, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependentPKA I and II(Kis of 12.5 µM and 4.5 µM, respectively) antagonist. Rp-cAMPS is resistant to hydrolysis by phosphodie...
YN480889 Apraclonidine hydrochloride 73218-79-8
Apraclonidine, also known as iopidine, is a sympathomimetic used in glaucoma therapy. It is an alpha2-adrenergic agonist.
YN250710 Mevastatin 73573-88-3
Mevastatin is a competitive inhibitor of HMG-Coenzyme A (HMG-CoA) reductase with a binding affinity 10,000 times greater than the HMG-CoA substrate itself.
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